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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Spencer, Ben Felix
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (14/14 displayed)
- 2024Ultimate charge transport regimes in doping-controlled graphene laminates: phonon-assisted processes revealed by the linear magnetoresistancecitations
- 2023Elucidating the mechanism of self healing in hydro gel lead halide perovskite composites for use in photovoltaic devices
- 2023Environment effects upon electrodeposition of thin film copper oxide nanomaterialscitations
- 2022Surface stability of ionic-liquid-passivated mixed-cation perovskite probed with in-situ photoelectron spectroscopycitations
- 2022High efficiency semitransparent perovskite solar cells containing 2D nanopore arrays deposited in a single stepcitations
- 2021Improving the Efficiency, Stability, and Adhesion of Perovskite Solar Cells Using Nanogel Additive Engineeringcitations
- 2021Inelastic background modelling applied to Hard X-ray Photoelectron Spectroscopy of deeply buried layers: a comparison of synchrotron and lab-based (9.25 keV) measurementscitations
- 2020Using soft polymer template engineering of mesoporous TiO2 scaffolds to increase perovskite grain size and solar cell efficiencycitations
- 2020PMMA-grafted graphene nanoplatelets to reinforce the mechanical and thermal properties of PMMA compositescitations
- 2020Quantitative Electro-Reduction of CO2 to Liquid Fuel over Electro-Synthesized Metal-Organic Frameworkscitations
- 2019Air-Stable Methylammonium Lead Iodide Perovskite Thin Films Fabricated via Aerosol-Assisted Chemical Vapor Deposition from a Pseudohalide Pb(SCN)2 Precursorcitations
- 2019Iodine adsorption in a redox-active metal-organic frameworkcitations
- 2019Accessing γ-Ga2S3 by solventless thermolysis of gallium xanthates: A low temperature limit for crystalline products?citations
- 2018Ambient-Air-Stable Inorganic Cs2SnI6 Double Perovskite Thin Films via Aerosol-Assisted Chemical Vapour Depositioncitations
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article
Using soft polymer template engineering of mesoporous TiO2 scaffolds to increase perovskite grain size and solar cell efficiency
Abstract
The mesoporous (meso)-TiO2 layer is a key component of high-efficiency perovskite solar cells (PSCs). Herein, pore size controllable meso-TiO2 layers are prepared using spin coating of commercial TiO2 nanoparticle (NP) paste with added soft polymer templates (SPT) followed by removal of the SPT at 500 °C. The SPTs consist of swollen crosslinked polymer colloids (microgels, MGs) or a commercial linear polymer (denoted as LIN). The MGs and LIN were comprised of the same polymer, which was poly(N-isopropylacrylamide) (PNIPAm). Large (L-MG) and small (S-MG) MG SPTs were employed to study the effect of the template size. The SPT approach enabled pore size engineering in one deposition step. The SPT/TiO2 nanoparticle films had pore sizes > 100 nm, whereas the average pore size was 37 nm for the control meso-TiO2 scaffold. The largest pore sizes were obtained using L-MG. SPT engineering increased the perovskite grain size in the same order as the SPT sizes: LIN <S-MG <L-MG and these grain sizes were larger than those obtained using the control. The power conversion efficiencies (PCEs) of the SPT/TiO2 devices were ∼20% higher than that for the control meso-TiO2 device and the PCE of the champion S-MG device was 18.8%. The PCE improvement is due to the increased grain size and more effective light harvesting of the SPT devices. The increased grain size was also responsible for the improved stability of the SPT/TiO2 devices. The SPT method used here is simple, scalable, and versatile and should also apply to other PSCs.